生物
电池极性
细胞生物学
上皮极性
莫辛
形态发生
粘合连接
顶膜
埃兹林
放射毒素
PDZ域
心尖缩窄
信号转导衔接蛋白
CDC42型
支架蛋白
跨膜蛋白
GTP酶
细胞骨架
信号转导
上皮
细胞
钙粘蛋白
遗传学
受体
基因
标识
DOI:10.1146/annurev-cellbio-092910-154033
摘要
Epithelial tissue formation and function requires the apical-basal polarization of individual epithelial cells. Apical polarity regulators (APRs) are an evolutionarily conserved group of key factors that govern polarity and several other aspects of epithelial differentiation. APRs compose a diverse set of molecules including a transmembrane protein (Crumbs), a serine/threonine kinase (aPKC), a lipid phosphatase (PTEN), a small GTPase (Cdc42), FERM domain proteins (Moesin, Yurt), and several adaptor or scaffolding proteins (Bazooka/Par3, Par6, Stardust, Patj). These proteins form a dynamic cooperative network that is engaged in negative-feedback regulation with basolateral polarity factors to set up the epithelial apical-basal axis. APRs support the formation of the apical junctional complex and the segregation of the junctional domain from the apical membrane. It is becoming increasingly clear that APRs interact with the cytoskeleton and vesicle trafficking machinery, regulate morphogenesis, and modulate epithelial cell growth and survival. Not surprisingly, APRs have multiple fundamental links to human diseases such as cancer and blindness.
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